Evidence map›Paper›PMID 38720939›Full record

ArticleInternational journal of nanomedicine2024

Innovative Vancomycin-Loaded Hydrogel-Based Systems - New Opportunities for the Antibiotic Therapy.

Aleksandra Florczyk, Aleksandra Krajcer, Kinga Wójcik, Joanna Lewandowska-Łańcucka

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Aleksandra FlorczykFaculty of Chemistry, Jagiellonian University, Kraków, Poland.ORCID 0000-0003-2988-8237
Aleksandra KrajcerFaculty of Chemistry, Jagiellonian University, Kraków, Poland.
Kinga WójcikFaculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland.
Joanna Lewandowska-ŁańcuckaFaculty of Chemistry, Jagiellonian University, Kraków, Poland.ORCID 0000-0002-5447-4936

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Surgical site infections pose a significant challenge for medical services. Systemic antibiotics may be insufficient in preventing bacterial biofilm development. With the local administration of antibiotics, it is easier to minimize possible complications, achieve drugs' higher concentration at the injured site, as well as provide their more sustained release. Therefore, the main objective of the proposed herein studies was the fabrication and characterization of innovative hydrogel-based composites for local vancomycin (VAN) therapy. Methods: Presented systems are composed of ionically gelled chitosan particles loaded with vancomycin, embedded into biomimetic collagen/chitosan/hyaluronic acid-based hydrogels crosslinked with genipin and freeze-dried to serve in a flake/disc-like form. VAN-loaded carriers were characterized for their size, stability, and encapsulation efficiency (EE) using dynamic light scattering technique, zeta potential measurements, and UV-Vis spectroscopy, respectively. The synthesized composites were tested in terms of their physicochemical and biological features. Results: Spherical structures with sizes of about 200 nm and encapsulation efficiencies reaching values of approximately 60% were obtained. It was found that the resulting particles exhibit stability over time. The antibacterial activity of the developed materials against Conclusion: It is expected that the developed herein system will enable direct delivery of the antibiotic at an exposed to infections surgical site, providing drugs sustained release and thus will reduce the risk of systemic toxicity. This strategy would both inhibit biofilm formation and accelerate the healing process.

Indexed as

Anti-Bacterial AgentsChitosanHydrogelsStaphylococcus aureusVancomycinBiofilmsCollagenDrug CarriersDrug LiberationHumansHyaluronic AcidMicrobial Sensitivity TestsParticle SizeSurgical Wound InfectionAnti-Bacterial AgentsChitosanCollagenDrug CarriersHyaluronic AcidHydrogelsVancomycinbiopolymerschitosan-based capsulesdelivery systemshydrogelsvancomycin

Identifiers

PMID38720939
PMCPMC11078026

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.